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Ryan P. Liegel, Ph.D.

Affiliations: 
2013 Cell Biology, Neurobiology, and Anatomy Medical College of Wisconsin, Milwaukee, WI, United States 
Area:
Genetics, Cell Biology, Molecular Biology
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"Ryan Liegel"
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Parents

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Duska Sidjanin grad student 2013 Medical College of Wisconsin
 (Genetic and molecular studies of the blind-sterile (bs) and blind-sterile 2 (bs2) mouse models of cataracts and male infertility.)
Rolf W. Stottmann post-doc Cincinnati Children's Hospital Medical Center (Neurotree)

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Publications

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Liegel RP, Michalski MN, Vaidya S, et al. (2023) Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformations. Development (Cambridge, England). 150
Bittermann E, Abdelhamed Z, Liegel RP, et al. (2019) Differential requirements of tubulin genes in mammalian forebrain development. Plos Genetics. 15: e1008243
Liegel RP, Finnerty E, Ward L, et al. (2018) Using human sequencing to guide craniofacial research. Genesis (New York, N.Y. : 2000)
Park AK, Liegel RP, Ronchetti A, et al. (2014) Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice. Bmc Genetics. 15: 135
Liegel RP, Ronchetti A, Sidjanin DJ. (2014) Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome. Molecular Genetics and Metabolism Reports. 1: 299-311
Liegel RP, Handley MT, Ronchetti A, et al. (2013) Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans. American Journal of Human Genetics. 93: 1001-14
Liang L, Liegel R, Endres B, et al. (2011) Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice. Molecular Vision. 17: 3062-71
Liegel R, Chang B, Dubielzig R, et al. (2011) Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice. Molecular Genetics and Metabolism. 103: 51-9
Hassemer EL, Le Gall SM, Liegel R, et al. (2010) The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17. Genetics. 185: 245-55
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